Canonical Allele Identifier: CA2172867039

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42725550G= , CM000677.2:g.42725550G=	GRCh38
NC_000015.9:g.43017748G= , CM000677.1:g.43017748G=	GRCh37
NC_000015.8:g.40805040G=	NCBI36
NG_012491.1:g.16670C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.3389C= MANE Select	ENSP00000348564.3:p.Pro1130=
ENST00000643434.1:c.*2456C=	ENSP00000494699.1:n.*2456C=
ENST00000356231.3:c.3389C=	ENSP00000348564.3:p.Pro1130=
ENST00000562465.5:c.1335C=	ENSP00000454246.1:n.1335C=
ENST00000563604.1:n.88C=
NM_138477.2:c.3389C=	NP_612486.2:p.Pro1130=
XM_005254176.3:c.3392C=	XP_005254233.1:p.Pro1131=
XM_011521270.1:c.3416C=	XP_011519572.1:p.Pro1139=
XM_011521271.1:c.3413C=	XP_011519573.1:p.Pro1138=
XM_011521274.1:c.2381C=	XP_011519576.1:p.Pro794=
XM_011521275.1:c.2633C=	XP_011519577.1:p.Pro878=
NM_138477.4:c.3389C= MANE Select	NP_612486.2:p.Pro1130=
XM_005254176.5:c.3392C=	XP_005254233.1:p.Pro1131=
XM_011521270.2:c.3416C=	XP_011519572.1:p.Pro1139=
XM_011521271.2:c.3413C=	XP_011519573.1:p.Pro1138=
XM_011521274.2:c.2381C=	XP_011519576.1:p.Pro794=
XR_001751104.1:n.3382C=
XR_001751105.1:n.3399C=